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Educational Intervention for Coping with Vision Loss

This study is looking at whether a brief audiovisual educational intervention can help people who are experiencing visual loss. The goal is to see if this intervention improves your awareness of shared experiences, like feelings of grief and isolation, that can come with vision loss. You would answer some questions, watch the educational material, and then answer more questions. The study aims to enroll 300 adults aged 18 to 89 who have recently visited a low-vision rehabilitation clinic. The study's status is currently unclear, so it's not known if they are actively recruiting.

Study design
This is an interventional study, meaning participants will receive a specific intervention. It plans to enroll 300 participants.
What's involved
You will be asked to answer questions, engage with an audiovisual educational intervention, and then answer additional questions. This will take place within about one week.
Compensation
Not stated in the trial record.
Follow-up
Your awareness will be measured from before the intervention to within one week after completing the post-intervention questions.

AI-generated from the public study record. Only the study team can confirm whether you're eligible — confirm details with them before making decisions.

NCT07715695

Evaluation of a Scalable Educational Intervention for Adjustment and Coping to Vision Loss

Enrolling by Invitation
NAAges 18–89Interventional
Brigham and Women's Hospital
~300 participants
Updated 2026-09-15 on ClinicalTrials.gov
What's tested:audiovisual educational intervention

At a glance

Recruiting sites
0 of 2 listed sites are recruiting right now
RecruitingSuspended, closed, or not yet open
What they're measuring
Change from Baseline in Educational Awareness of Shared Themes as Measured by Likert-scale Questions
Measured over From baseline to completion of post-intervention questions (e.g., within 1 week).

Conditions

Visual Loss

Explore related trials

Loss of Vision

NCT07715695

Where you'd take part

This study runs at 2 sites. They're the same protocol — you choose where, and that choice sets who your contact draft is addressed to.

  • Brigham and Women's Hospital, Mass General Brigham

    Boston, Massachusettsno site contact published

  • New England College of Optometry

    Boston, Massachusettsno site contact published

Sites open and close at different times, so the status above is per site — it can differ from the study's overall status.

Study leadership

  • Ali S Raza, MD, PhD · PRINCIPAL_INVESTIGATOR · Brigham and Women's Hospital, Mass General Brigham

Who to contact

This trial hasn't published a contact. View it on ClinicalTrials.gov

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Eligibility criteria

Inclusion

have capacity to provide informed consent
have had a visit within a low-vision rehabilitation clinic

Exclusion

are unable to engage with the audiovisual educational intervention

What this trial measures

  • Change from Baseline in Educational Awareness of Shared Themes as Measured by Likert-scale QuestionsFrom baseline to completion of post-intervention questions (e.g., within 1 week).

    Higher values (or increases relative to baseline) correspond to better outcomes, with each question having a minimum value of 1 and a maximum value of 5.